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Earlier this month Therapeutic Coach Samantha Quemby joined Morven-May MacCallum on LDUK Connect.

An edited recording of this session is now available for those who were unable to attend.

lymediseaseuk.com/healing-your...

#Lyme #lymewarrior #lymedisease #lymeadvocate #lymeawareness

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I’m still fighting. 3 years of Lyme but progressively worse since June. Mine manifests with extraordinary chronic pain. Then we are all watching our country fall apart daily. My soul can’t breathe. I want to breathe… #lymedisease #lymewarrior

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Breathe deep in fresh air when you can all the way into your belly. It will help with brain energy and clearing your mind even for a moment. Then it helps you detox harmful things from your body. Just breathe. #sanskrit #lymewarrior

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Lyme disease case rates are increasing faster in other NE states In 2010, Connecticut had the second-highest Lyme disease case rate in New England. In 2023, it had the lowest.

Cred: @renatadaou.bsky.social @ctmirror.org

#lyme #lymedisease #lymediseaseawareness #lymewarrior #chronicillness #chroniclyme #lymelife #chroniclymedisease #invisibleillness #chronicpain #lymesucks #lymetreatment #autoimmunedisease #lymestrong #chronicfatigue #lymefighter

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And I forgot the #LymeWarrior so I have to go back. And I want to change pic to something current. It wasn’t hard at all.

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5 myths about Lyme disease…
5 myths about Lyme disease… YouTube video by Talia Smith - Finding Vulneraries

In honor of Lyme Disease Awareness Month, here are 5 myths about Lyme Disease.
#myths #lymedisease #lyme #lymediseaseawareness #awareness #didyouknow #factsyoudidntknow #lymewarrior #chroniclyme #ChronicLymeDisease

youtube.com/shorts/9Ze4i...

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Were you dismissed like my first Lyme disease patients? Share your story below. #LymeDisease #LymeAwareness #ChronicLyme #LymeDoctor #LymeWarrior #TickBorneIllness #MedicalJourney #PatientStory #case #explainer #lymephysician

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May is Lyme Disease Awareness Month.
May is Lyme Disease Awareness Month. YouTube video by Talia Smith - Finding Vulneraries

In honor of May also being #LymeDiseaseAwarenessMonth here is a video discussing common misconceptions about testing and diagnosis. #Lyme #lymedisease #lymewarrior #LymeDiseaseAwareness #factsyoudidntknow #DidYouKnow

igenex.com

youtube.com/shorts/LJ7x4...

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Today and every day, we celebrate the incredible strength, love, and resilience of all moms—especially those fighting for the health of their children.
Happy Mother’s Day from all of us at the LivLyme Foundation. Thank you for never giving up. 💚💐

#MothersDay #LymeMoms #LivLyme #LymeWarrior #Thanku

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About the Center : Johns Hopkins Medicine Lyme Disease Research Center The Johns Hopkins Medicine Lyme Disease Research Center was established in 2015 under the direction of John Aucott, MD. Our clinical research team sees patients at Johns Hopkins at Green […]

May is #LymeDisease Awareness Month. Visit Johns Hopkins Lyme Disease Research Center. Learn the truth about one of the fastest growing epidemics in the world. Support them. Subscribe to their newsletter. #LymeWarrior #LymeDiseaseAwareness www.hopkinslyme.org/about-the-ce...

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Photo of a key lime pie on a cooling rack

Photo of a key lime pie on a cooling rack

A slice of key lime pie on a plate behind a fork

A slice of key lime pie on a plate behind a fork

My partner once again made me a key lime pie for my (not key) lyme anniversary (9 years today)

It was scrumptious 🤤

#LymeDisease #lyme #LymeWarrior #FuckLyme #LymeAnniversary #KeyLimePie

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Italian greyhound Kira and her mommy enjoying sunshine.

Italian greyhound Kira and her mommy enjoying sunshine.

Beautiful day, Kira and I are enjoying a little bit of sunshine. It's sad that a primary thing on my mind, as I enjoy a few minutes of outdoors, is whether or not we're picking up ticks. #LymeDisease #LymeWarrior #DogsOfBlueSky #ItalianGreyhound

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Johns Hopkins Lyme Disease Research Center. Here is their current newsletter issue, in PDF format. Visit them at hopkinslyme [dot] org. #ChronicLyme #LymeDisease #LymeWarrior #LymeDiseaseResearch #JohnsHopkins

www.hopkinslyme.org/wp-content/u...

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Love and light to anyone feeling alone or trapped.

I have survived things I could’ve never imagined.

You have, too, I bet.

Now is our time to thrive in ways we’ve never imagined—

at least not yet.

#lymewarrior

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CDC budget cuts affect Lyme disease research at Fort Collins | LymeDisease.org In a February 20 Facebook post, Dr. Richard Horowitz relates: "Many of the epidemiologists at the CDC in Fort Collins, working on tick-borne diseases were

"Many of the epidemiologists at the CDC in Fort Collins, working on tick-borne diseases were just fired. "

#lymedisease #lymewarrior #chroniclyme

www.lymedisease.org/cdc-budget-c...

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#lymewarrior

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A white ramekin on a wooden table, filled with 18 pills in varying shapes, sizes, and colors

A white ramekin on a wooden table, filled with 18 pills in varying shapes, sizes, and colors

Mmm, breakfast

These are all the meds (all supplements) I take with breakfast every day. None of these fight lyme, but almost all are because of lyme

#ThatChronicIllnessLife #ChronicIllness #LymeDisease #Lyme #disabilitysky #disabledsky #lymesky #ThatLymeLife #medicine #LymeEducation #LymeWarrior

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Ran out of room but wanted to include #LymeDisease #LymeWarrior #lymesky and #FuckLyme

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A woman in a kn95 mask and face shield getting an IV and holding out 3 fingers. She's wearing a black t-shirt with a grizzly bear in am astronaut's space suit and space themed yoga oanys

A woman in a kn95 mask and face shield getting an IV and holding out 3 fingers. She's wearing a black t-shirt with a grizzly bear in am astronaut's space suit and space themed yoga oanys

I'm currently doing an unusual, RNA based lyme treatment instead of antibiotics (like I've done for the last 8.5 years)

Today was IV #3

I really hope these work

#LymeWarrior #lyme #LymeDisease #FuckLyme #disabled #disability #ChronicallyIll #DisablitiySky #LymeSky

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🌿 Your story matters!

Are you a Lyme disease patient or caregiver? Sharing your journey could raise awareness, support others, and inspire change.

💚 Submit your story here:

👉 lymediseaseuk.com/contact-us/s...

#LymeDiseaseAwareness #ShareYourStory #LymeWarrior

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I desperately want my life back. I’m a shell of the person I once was.

I’m holding onto every glimpse of hope that I’ll finally heal.

#lymedisease #lymeawareness #lymewarrior #MECFS #CIRS #mentalhealth #PTSD #anxiety #chronicillness #hope

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I now fully understand why patients of #lymedisease use the term #lymewarrior.

It feels like my body is legit trying to take me out and I’m not even close to being on the #Lyme protocol yet. My body was too sensitive for the gentle treatment, so now we move to what they give children.

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Mixed emotions about how, but Lyme Disease is now on the national stage 💚 hopefully it makes a change in the way the medical industry views/handles it
#lymedisease #lymewarrior #lyme #chroniclyme

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No matter how many times #moldtoxicity & #lymedisease knock me down... I'll still keep fighting in bed 💪❤️

I'm a #LymeWarrior ‼️🍋‍🟩

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A poster with a dark turquoise background and bullet points of the 10 principles of disability justice.

A poster with a dark turquoise background and bullet points of the 10 principles of disability justice.

#ableism #medicalgaslighting
#medicalmisogyny #mydisabledlifeisworthy
#actuallyautistic #chronicallyawesome #lymewarrior #disabilityjustice #healthcare #captalismkills #collectiveliberation #intersectionality #bodyautonomy

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Poster with a turquoise background and yellow and white text describing manifestations of ableism. These include “internalized”, “interpersonal”, and “institutional”.

Poster with a turquoise background and yellow and white text describing manifestations of ableism. These include “internalized”, “interpersonal”, and “institutional”.

#ableism #medicalgaslighting #medicalmisogyny #mydisabledlifeisworthy #actuallyautistic #chronicallyawesome #lymewarrior #disabilityjustice #healthcare

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Screen shot of texts of my friend calling me a goose after I confess to her that one of the reasons I can't learn piano, besides my progressive illness and disability is that I don't actually own a piano

Screen shot of texts of my friend calling me a goose after I confess to her that one of the reasons I can't learn piano, besides my progressive illness and disability is that I don't actually own a piano

This is why I love my friends. They make me laugh. They keep it real. And that helps me cope with life much better. I think I will stick to listening to piano music while writing books! Life is short, and I need to prioritize. 3/3 #lymewarrior #chronicillness #music #disability #chronicillnesshumor

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I've got something to say! The people who suffer from this disease are TIRED! Please repost and share this with someone who needs it!
Tap the link to stream the full song now!!

FFO:
Linkin Park
Architects
Motionless In white
Ect

#LymeWarrior #NuMetal #Metalcore

open.spotify.com/track/33MrSo...

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My GF has been suffering from Lyme Disease since 2018, so I wrote a song to bring awareness in hopes it goes viral, so we can afford treatment, please tap the link to give this song a listen 🤘🏻
distrokid.com/hyperfollow/...

#Metalcore #Metalmusic #LymeWarrior #ChronicLyme #NuMetal #AlbumArt #HipHop

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Lyme and Reason:  Dr. Neil Spector
Lyme and Reason: Dr. Neil Spector Renowned Oncologist Neil Spector, MD shares his own personal story of his transition from doctor to patient, and how Lyme disease led to an emergency heart t...

An interview from 2016 with Dr. Neil Spector, prominent oncologist and researcher, whose misdiagosis cost him his heart and, in 2020, his life. Lyme Disease Carditis: his doctors wouldn't listen until it was too late. Please watch.
#LymeDisease
#LymeWarrior

www.youtube.com/watch?v=Ja9i...

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